Assessing urinary biomarkers in membranous glomerulonephritis
Official title: Correlation and Clinical Utility of Urinary Biomarker in Membranous Glomerulonephritis
Run by Chinese University of Hong Kong · NCT05688865 · Data updated 2026-11-12
This study is testing if urine samples can provide useful information about kidney health in people who have just been diagnosed with membranous glomerulonephritis.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 50 (estimated) |
| Sponsor | Chinese University of Hong Kong Academic / other |
| Locations | 1 site (Shatin) |
| Status | Recruiting |
| Started | February 1, 2023 |
| Main results expected | December 31, 2026 |
| Study ends | December 31, 2026 |
| Registry record updated | October 21, 2026 |
| Trial ID | NCT05688865 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are individuals with newly diagnosed biopsy-proven primary membranous glomerulonephritis.
✕Probably not a fit
Patients with secondary causes of membranous nephropathy, such as lupus nephritis or viral hepatitis, may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study aims to evaluate the correlation between urinary biomarkers and serum samples in patients with newly diagnosed membranous glomerulonephritis (MGN). Fifty patients will be recruited and followed for one year, during which serum and urinary biomarkers will be collected every four months and analyzed using ELISA assays. The primary outcome is to determine the correlation of urinary biomarkers with serum markers, while secondary outcomes include their relationship with clinical parameters such as eGFR decline and renal events. This research seeks to establish the clinical utility of urinary biomarkers as a non-invasive alternative to serum samples.
Why it matters
Potential benefit: If successful, this study could provide a non-invasive method for detecting and monitoring membranous glomerulonephritis.
How similar studies have gone: While the use of serum biomarkers has been established, the clinical utility of urinary biomarkers in this context is still being explored, making this approach relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * newly diagnosed biopsy proven primary membranous glomerulonephritis Exclusion Criteria: * secondary causes of membranous nephropathy, e.g. lupus nephritis, viral hepatitis B and C and malignancy
Where it's running
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Department of Medicine & Therapeutics, Prince of Wales Hospital
Shatin, Hong Kong Recruiting
Study contacts
- Study coordinator: Winston WS Fung, MBBS
- Email: fws898@ha.org.hk
- Phone: 35053528
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Rituximab plus Cyclosporine for Primary Membranous Nephropathy
This study tests whether adding Cyclosporine to Rituximab helps people with primary membranous nephropathy achieve remission of heavy protein in the urine faster.
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This trial will test whether adding HLX79 at different doses to rituximab (HLX01) helps adults with active membranous nephropathy or lupus nephritis.
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This study is testing if a new oral treatment called ManNAc can help adults with kidney disease FSGS by reducing protein levels in their urine and checking how safe it is over 12 weeks.
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AI-guided personalized rituximab for membranous nephropathy
This trial will test whether an AI-guided approach to dosing rituximab improves remission in adults with PLA2R1-positive nephrotic membranous nephropathy.
-
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This project will follow adults with primary membranous nephropathy and nephrotic syndrome to see how their disease and real-world treatments affect long-term kidney outcomes.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.